Search results for "MR"

showing 10 items of 3001 documents

Binding Profiles of Self-Assembled Supramolecular Cages from ESI-MS Based Methodology

2018

Confined molecular environments have peculiar characteristics that make their properties unique in the field of biological and chemical sciences. In recent years, advances in supramolecular capsule and cage synthesis have presented the possibility to interpret the principles behind their self‐assembly and functions, which has led to new molecular systems that display outstanding properties in molecular recognition and catalysis. Herein, we report a rapid method based on ESI‐MS to determine the binding profiles for linear saturated dicarboxylic acids in a series of different cages. The cages were obtained by self‐assembly of modified tris(pyridylmethyl)amine (TPMA) complexes and diamines cho…

cage compounds; dynamic covalent chemistry; molecular recognition; supramolecular chemistry; tris(pyridylmethyl)amine; Chemistry (all)Electrospray ionizationSupramolecular chemistry010402 general chemistry01 natural sciencesCatalysissupramolecular chemistryParamagnetismMolecular recognitionComputational chemistrysupramolekulaarinen kemiaSettore CHIM/01 - Chimica AnaliticaSpectroscopyta116010405 organic chemistryChemistryOrganic ChemistryChemistry (all)Dynamic covalent chemistrySettore CHIM/06 - Chimica OrganicaGeneral Chemistry0104 chemical sciencesProton NMRtris(pyridylmethyl)amineAmine gas treatingdynamic covalent chemistrymolecular recognitioncage compounds
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Hyper-reticulated calixarene polymers: a new example of entirely synthetic nanosponge materials

2018

New calixarene-based nanosponges (CaNSs), i.e., hyper-reticulated polymers constituted by calixarene monomer units joined by means of bis(1,2,3-trialzolyl)alkyl linkers, were synthesized, characterized and subjected to preliminary tests to assess their supramolecular absorption abilities towards a set of suitable organic guests, selected as pollutant models. The synthesis was accomplished by means of a CuAAC reaction between a tetrakis(propargyloxy)calix[4]arene and an alkyl diazide. The formation of the polymeric network was assessed by means of FTIR and 13C{1H} CP-MAS solid-state NMR techniques, whereas morphological characterization was provided by SEM microghaphy. The materials were pro…

calixarenesSupramolecular chemistrynanosponges02 engineering and technology010402 general chemistryNanosponge01 natural sciencesFull Research PaperHydrophobic effectlcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistrySmart materialCalixarenePolymer chemistryFourier transform infrared spectroscopylcsh:ScienceAlkylSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationOrganic ChemistrySettore CHIM/06 - Chimica OrganicaSettore CHIM/05 - Scienza E Tecnologia Dei Materiali PolimericiPolymer021001 nanoscience & nanotechnology0104 chemical sciencesChemistryMonomerchemistrySolid-state nuclear magnetic resonancesmart materialsCalixarenesolid-state NMRlcsh:Q0210 nano-technologyBeilstein Journal of Organic Chemistry
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Poly-iodinated closo 1,2-C 2 B 10 and nido [7,8-C 2 B 9 ] − carborane frameworks: Synthesis and consequences

2015

Abstract The preparation of Cc-monosubstituted closo and nido carborane derivatives, mono-, di and tetraiodinated is reported. Some of these mono-to poly-iodinated nido carboranes are studied in terms of the acidity of the open face bridging proton, their chemical shift position in the 1H NMR, and the lesser tendency to η5-coordination in parallel to a larger number of iodo groups.

carboranesSolvent freeStereochemistryChemistryOrganic ChemistryHalogenationsolvent freeBiochemistryInorganic ChemistryiodinationMaterials ChemistryProton NMRCarboranePhysical and Theoretical Chemistryta116acidityJournal of Organometallic Chemistry
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Dynamic Stabilization of the Ligand-Metal Interface in Atomically Precise Gold Nanoclusters Au68 and Au144 Protected by meta-Mercaptobenzoic Acid

2017

Ligand-stabilized, atomically precise gold nanoclusters with a metal core of a uniform size of just 1–3 nm constitute an interesting class of nanomaterials with versatile possibilities for applications due to their size-dependent properties and modifiable ligand layers. The key to extending the usability of the clusters in applications is to understand the chemical bonding in the ligand layer as a function of cluster size and ligand structure. Previously, it has been shown that monodispersed gold nanoclusters, stabilized by meta-mercaptobenzoic acid (m-MBA or 3-MBA) ligands and with sizes of 68–144 gold atoms, show ambient stability. Here we show that a combination of nuclear magnetic reson…

carboxylic acidsspectroscopyGeneral Physics and AstronomyInfrared spectroscopyNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesNanoclustersNanomaterialsMetalMolecular dynamicsNMR spectroscopyGeneral Materials Scienceclustersta116thiolsta114LigandChemistryGeneral Engineeringgold021001 nanoscience & nanotechnologymolecular dynamicsvibrational spectroscopy0104 chemical sciencesCrystallographyChemical bondgold nanoclustervisual_artvisual_art.visual_art_mediumDensity functional theory0210 nano-technologyACS Nano
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Large Mediastinal mass in pregnancy: utility of echocardiography and cardiac MRI. A case report

2011

cardiac MRIechocardiographypregnancylarge mediastinal ma
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EVALUATION OF INORGANIC CONTAMINANT REMOVAL FROM AQUEOUS SOLUTIONS USING PYROLIZED CHICKEN MANURE, CONIFER AND POPLAR WOOD AS ADSORBENT

2014

Anthropogenic activities alter the natural flow of materials and introduce novel chemicals into the environment thereby causing serious soil and water pollution. Indeed, many industries produce aqueous effluents containing toxic substances, especially heavymetals. The presence of these contaminants in the environment is a great issue because of their toxicityand bioaccumulation ability which affect human life and the environment. Various physicochemical and biological techniques have been used to remove the heavy metals from waste waters, including chemical precipitation, ion exchange, chemical coagulation, electrolytic methods, membrane processes, and adsorption. Biochar is a carbonaceous …

char heavy metal adsorption nmr
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Sodium ions models cheeses at molecular and macroscopic levels

2009

National audience; The excessive consumption of sodium is one of the causes of nutritional related-health problems. The reduction of salt content without affecting technological and sensorial properties of foodstuffs is currently a challenge for the food industry1. There is a need to develop tools to quantify the “active” sodium ions in food products at molecular and macroscopic levels to better understand in-mouth salt release and flavour perception. In this context, methods for the quantification of the bound fraction were developed: 23Na NMR single-quantum (SQ) and double-quantum-filtered (DQF) sequences at molecular level using Bruker Avance-500 spectrometer equipped with 10 mm probe 2,…

cheese[SPI.GPROC] Engineering Sciences [physics]/Chemical and Process Engineering[SDV.IDA]Life Sciences [q-bio]/Food engineering[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process Engineering[SDV.IDA] Life Sciences [q-bio]/Food engineeringsodiumnmr
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Field-induced slow relaxation of magnetization in a mononuclear Co(II) complex of 2,6-bis(pyrazol-1-yl)pyridine functionalized with a carboxylic acid

2018

Abstract Combining Co(II) with the 2,6-bis-(pyrazol1-yl)pyridine ligand functionalized with a carboxylic acid group (bppCOOH) results in the compound [CoII(bppCOOH)2](ClO4)2·2Me2CO, which shows a field-induced slow relaxation of magnetization as a result of the magnetic anisotropy of the distorted octahedral coordination of high-spin Co(II). Co(II)/Fe(II) solid solutions of bppCOOH have been prepared to study the influence of Co(II) on the spin crossover properties of Fe(II). Magnetic characterization of [Fe0.92Co0.08(bppCOOH)2](ClO4)2 indicates that the Cobalt dopant leads to a reduction of T1/2 and a loss of cooperativity of the spin transition.

chemistry.chemical_classification010405 organic chemistryCarboxylic acidRelaxation (NMR)Spin transitionchemistry.chemical_element010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryCrystallographyMagnetizationchemistry.chemical_compoundMagnetic anisotropychemistrySpin crossoverPyridineMaterials ChemistryPhysical and Theoretical ChemistryCobaltPolyhedron
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Supramolecular complexes formed by dimethoxypillar[5]arenes and imidazolium salts: A joint experimental and computational investigation

2017

To gain more insights into the factors acting on the stability of complexes formed by pillar[5]arenes, we investigated the interaction of dimethoxypillar[5]arene with some 1-(n-alkyl)-3-(9-anthracenylmethyl)-imidazolium based organic salts. In particular, we used salts differing in not only the anion nature ([Cl−], [BF4−], [NTf2−] and [SbF6−]) and alkyl chain length (butyl, octyl and dodecylimidazolium derivatives), but also the presence of a hydrogenated or fluorinated tail (octyl and perfluorooctylimidazolium derivatives). Host–guest systems were analysed in solution, solid state and gas phase, using a combined approach of different techniques like fluorescence, 1H NMR, ESI-MS, DSC and DF…

chemistry.chemical_classification010405 organic chemistryChemistryInorganic chemistrySupramolecular chemistrySolid-stateGeneral ChemistrySettore CHIM/06 - Chimica Organica010402 general chemistry01 natural sciencesFluorescenceCatalysis0104 chemical sciencesIonSolventimidazolium salt.CrystallographyChain lengthMaterials ChemistryProton NMRpillar[5]areneAlkylSupramoleculr chemistry
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Synthesis, X-ray structure, Hirshfeld analysis, and DFT studies of a new Pd(II) complex with an anionic s-triazine NNO donor ligand

2020

Abstract A new Pd(II) complex, [Pd(Triaz)Cl], with the hydrazono-s-triazine ligand, 2,4-di-tert-butyl-6-((2-(4-morpholino-6-(phenylamino)-1,3,5-triazin-2-yl)hydrazono)methyl)phenol (HTriaz), was synthesized by the reaction of PdCl2 with the organic ligand (1:1) in acetone under isothermal conditions. The molecular structure of the [Pd(Triaz)Cl] complex was determined using FTIR and 1H NMR spectroscopic techniques, and single-crystal X-ray diffraction. Moreover, using Hirshfeld surface analysis, the percentages of the intermolecular interactions were determined. The obtained values were 60.6%, 11.6%, 8.1%, 3.6%, and 5.0% for the H⋯H, C⋯H, O⋯H, N⋯H, and Cl⋯H interactions, respectively. Among …

chemistry.chemical_classification010405 organic chemistryChemistryLigandOrganic ChemistryIntermolecular forceHydrazone010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryInorganic ChemistryCrystallographychemistry.chemical_compoundElectron transferProton NMRMoleculeSpectroscopyTriazineNatural bond orbitalJournal of Molecular Structure
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